Cat.No.: | PE-0786 |
Product Name: | Recombinant Human ATRX protein, GST-tagged |
Product Overview: | Recombinant Human ATRX(1 a.a. - 90 a.a.) fused with GST tag at N-terminal was expressed in Wheat Germ. |
Description: | The protein encoded by this gene contains an ATPase/helicase domain, and thus it belongs to the SWI/SNF family of chromatin remodeling proteins. The mutations of this gene are associated with an X-linked mental retardation (XLMR) syndrome most often accompanied by alpha-thalassemia (ATRX) syndrome. These mutations have been shown to cause diverse changes in the pattern of DNA methylation, which may provide a link between chromatin remodeling, DNA methylation, and gene expression in developmental processes. This protein is found to undergo cell cycle-dependent phosphorylation, which regulates its nuclear matrix and chromatin association, and suggests its involvement in the gene regulation at interphase and chromosomal segregation in mitosis. Multiple alternatively spliced transcript variants encoding distinct isoforms have been reported. |
Applications: | Enzyme-linked Immunoabsorbent; Assay Western Blot (Recombinant protein); Antibody Production; Protein Array |
Storage: | Store at 4℃ if entire vial will be used within 2-4 weeks. Store at -20℃ or -80℃ for longer periods of time. Avoid multiple freeze-thaw cycles. |
Molecular Weight: | 35.53 kDa |
Species: | Human |
Formulation: | 50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer. |
Tag: | GST |
Amino Acid Sequence: | MTAEPMSESKLNTLVQKLHDFLAHSSEESEETSSPPRLAMNQNTDKISGSGSNSDMMENSKEEGTSSSEKSKSSG SSRSKRKPSIVNKND |
Expression System: | Wheat Germ |
Protein Length: | 1 a.a. - 90 a.a. |
Warning: | This product is for research use only. Not for use in diagnostic or therapeutic procedures. |
Gene Name: | ATRX alpha thalassemia/mental retardation syndrome X-linked [ Homo sapiens ] |
Gene ID NCBI: | 546 |
Official Symbol: | ATRX |
Synonyms: | ATRX; alpha thalassemia/mental retardation syndrome X-linked; alpha thalassemia/mental retardation syndrome X linked (RAD54 (S. cerevisiae) homolog) , JMS, Juberg Marsidi syndrome , RAD54; transcriptional regulator ATRX; RAD54 homolog (S. cerevisiae); XH2; XNP; RAD54 homolog; X-linked helicase II; Zinc finger helicase; helicase 2, X-linked; X-linked nuclear protein; ATP-dependent helicase ATRX; DNA dependent ATPase and helicase; alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S. cerevisiae); JMS; SHS; ATR2; SFM1; RAD54; MRXHF1; RAD54L; ZNF-HX; MGC2094; |
mRNA Refseq: | NM_000489 |
Protein Refseq: | NP_000480 |
MIM: | 300032 |
UniProt ID: | P46100 |
Chromosome Location: | Xq21.1 |
Function: | ATP binding; DNA binding; DNA helicase activity; chromatin binding; chromo shadow domain binding; helicase activity; hydrolase activity; metal ion binding; nucleotide binding; protein binding; zinc ion binding; |
Product Types | ||
◆ Cell Lines | ||
CL-0020 | Human ATAD2 Knockout Cell Line 2bp deletion | Inquiry |
CL-0021 | Human ATAD2B Knockout Cell Line 130bp insertion | Inquiry |
CL-0022 | Human ATAD2B Knockout Cell Line 130bp insertion | Inquiry |
◆ Research Kits | ||
EKIT-0021 | ATF2 (pT69/pT71) Transcription Factor Assay Kit | Inquiry |
◆ Extracts & Lysates | ||
EL-0031 | Recombinant Human ATAD2 293 Cell Lysate | Inquiry |
Related Gene / Proteins | |||
ATAD2 | ATAT1 | ATF-6 | ATF1 |
ATF2 | ATF4 | ATM | ATR |
ATRX | ATXN3 | ATXN3L | ATXN7 |
ATXN7L3 |
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